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2-BROMOETHYLAMINE HYDROCHLORIDE → HCID 54585665, 화합물

HRID 364185
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HRID 364185 반응식
[NH2:1][C:2]1[CH:10]=[CH:9][C:8]2[N:7]([CH2:11][CH2:12][N:13]([CH2:16][CH3:17])[CH2:14][CH3:15])[N:6]=[C:5]3[C:18]4[CH:24]=[CH:23][CH:22]=[CH:21][C:19]=4[S:20][C:3]=1[C:4]=23.Cl.[Br:26][CH2:27][CH2:28][NH2:29]>CCO>[BrH:26].[CH2:14]([N:13]([CH2:16][CH3:17])[CH2:12][CH2:11][N:7]1[C:8]2[CH:9]=[CH:10][C:2]([NH:1][CH2:27][CH2:28][NH2:29])=[C:3]3[S:20][C:19]4[CH:21]=[CH:22][CH:23]=[CH:24][C:18]=4[C:5]([C:4]=23)=[N:6]1)[CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 122086202-BROMOETHYLAMINE HYDROCHLORIDEHCID 13689033HCID 13689033, 화합물

생성물 1

HCID 54585665HCID 54585665, 화합물수율 37.5%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 5.0 g (0.015 mol) of 5-amino-N,N-diethyl-2H[1]benzothiopyrano[4,3,2-cd]indazole-2-ethanamine and 9.2 g (0.045 mol) of 2-bromoethylamine, hydrochloride in 50 ml of EtOH was heated under reflux for four days and allowed to cool to room temperature. The solid was collected and recrystallized from MeOH to give 2.6 g of product, mp 263° C. dec.

후처리

  1. temperatureunder reflux for four days
  2. customThe solid was collected
  3. customrecrystallized from MeOH

출처 및 근거

ORD 기록
ord-2ff49878ebf94ee5baacf63be9912c73
출처 데이터셋
uspto-grants-1986_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04604390

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